Preparation and use of radium-223 to target calcified tissues for pain palliation, bone cancer therapy, and bone surface conditioning

ABSTRACT

Processes for the preparation, prepared solutions, and the use of radium- 223  for the treatment of calcified tumors, bone tumors, treatment of bones, bone surfaces and soft tissues is described.

[0001] The present invention relates to the preparation and use of the “calcium analogue” alkaline-earth radionuclide radium-223 for the targeting of calcified tissues, e.g., bone and a physiological acceptable solution comprising ²²³Ra.

[0002] Biomedical use of radionuclides for pain palliation and/or cancer treatment, including prophylactic treatment of bone surfaces to slow down/inactivate undetectable metastases has previously been based upon β-emitters and conversion electron emitters.

[0003] A substantial percentage of cancer patients is affected by skeletal metastases. As many as 85% of patients with advanced lung, prostate and breast carcinoma develop bony metastases (Garret, 1993; Nielsen et al., 1991). Established treatments such as hormone therapy, chemotherapy and external radiotherapy often causes temporary responses, but ultimately most bone cancer patients experience relapses (Kanis, 1995). There is thus a strong need for new therapies to relieve pain and slow down tumor progression. Bone targeting radioisotopes has been included in clinical trials for the treatment of cancer to the skeleton (De Klerk et al., 1992, Foss{dot over (a)} et al., 1992, Lee et al., 1996, Silberstein, 1996). These radiopharmaceuticals have been based on β-particle emitters (Atkins, 1998) and lately also a conversion electron ermitter (Atkins et al., 1995). Among these compounds which have so far been approved by US Food and Drug Administration, Le., are strontium-89 (Metastron™) and ¹⁵³Sm EDTMP (Lexidronam™). The strontium-89 compound can only be administered in amounts sufficient for pain palliation, not for tumor therapy, because a significant myelotoxicity occurs before significant antitumour therapeutic dose levels can be reached (Silberman, 1996).

[0004] Recently, one of the inventors authored a publication (Larsen et al., 1999) showing by dosimetry that α-emitters can be more advantageous than β-emitters as bone seekers. I.e. the shorter range of the α-emitters effecting less bone marrow exposure when the source is located at bone surfaces. In this study two α-emitting bisphosphonate bone seekers were compared with two β-emitting compounds with similar chemical structures and bone affinity. Dosimetric calculations indicated that, in mice, the bone surface to bone marrow dose ratios were approximately 3 times higher with the α-emitter compared to the β-emitter. This indicates that α-emitting bone seekers may have advantages over β- and/or electron emitting compounds because the radiation dose can be more strongly concentrated to the bone surfaces. Because of the short half life (t_(1/2)=7.2 h) and since its production is limited to only a few sites worldwide, astatine-211 is at present not yet available for large scale marketing.

[0005] Besides astatine-211 only a few α-particle emitting radioisotopes are at present considered useful for biomedical applications (Feinendegen et al., 1997). The lead-212/bismuth-212 system has previously been used for preparation of bone seeking agents. Bismuth-212 complexed with ethylene-diamine-tetra(methylene-phosphonic acid) (EDTMP), or 1,4,7,10-tetraazacyclododecane 1,4,7,10-tetra(methylene-phosphonic acid) (DOTMP), showed a significant bone affinity. But because of the short half life of bismuth-212 (t_(1/2)=60.6 min), normal tissue exposure during the uptake phase of the radiopharmaceutical would be considerable (Hassfjell et al., 1994, 1997). This would be ever more pronounced with the other α-emitting bismuth isotope considered for biomedical use, the bismuth-213 (t ½=46 min). Attempts have been made to use the β-emitter lead-212 (t_(1/2)=10.6 h) as an in vivo generator for ²¹²Bi. However, a significant translocation affecting a high kidney accumulation of the α-emitter was observed (Hassfjell et al., 1997). Other α-emitting radioisotopes potentially useful for biomedical applications are the radium isotopes 224 and 226. As with other group 11 alkaline-earth metals, radium in its cationic state is a natural boneseeker.

[0006] Previously the radium isotopes 224 and 226 has been studied, partly because of their bone affinity (Loyd et al., 1982, 1991; Muggenburg et al., 1996, Muller, 1971; Raabe et al., 1993; Rundo, 1978). Radium-226 is, because of its long half-life (1600 years) and its noble gas radon-222 daughter (t_(1/2)=3.8 days), not considered useful for targeted radionuclide therapy. Because of its chemical nature, radon is inert to chemical bonding under in vivo conditions. It can therefore readily translocate in vivo when generated from the decay of the mother nuclide (Rundo, 1978). Inhaled radon mainly dissolves in body fluid and fat and is mainly eliminated from the body by exhalation (Rundo, 1978). In an experiment using bone samples, Lloyd and Bruenger (1991) reported that 89.5-94.25% of the radon-222 escaped from the bone after radium-226 had been administered to dogs. In contrast to radium-226, radium-224 has a half life (t_(1/2)=3.64 days) which seems very suitable for biomedical applications. ²²⁴Ra was used medically for many years to treat ankylosing spondylitis (Delikan, 1978). Unfortunately, also a significant fraction of the daughter isotopes of radium-224 escaped from bone, probably mainly because of the radon-220 (t_(1/2) of 55.6 s) daughter (Lloyd et al., 1982; Müller et al., 1971; Rundo, 1978).

[0007] It is thus known from previous studies that when the radium isotopes ²²⁴Ra and ²²⁶Ra were incorporated in bone, a significant translocalisation of their radon daughters occurred, which could, at least partly, explain the known carcinogenic effect of these two radium isotopes. This may be one of the reasons why α-emitters have not been evaluated clinically as bone seeking radiopharmaceutical against skeletal cancers.

[0008] It is the object of the present invention to provide a bone seeking radionuclide useful as a pharmaceutical agent, showing that radioactive decay products from its transformation do not translocalize significantly after its incorporation in bone (valid at least after 3 days from administration).

[0009] The present inventors made the significant and somewhat unexpected discovery that from ²²³Ra localized in bone, very little translocation of the radon daughter (as well as other radionuclides from the decay chain) occurred. Hence, the ²²³Ra series may be used to irradiate the bone surface without any significant translocation of radionuclides (including diffusion into bone marrow). Furthermore radium-223, should be more suitable as a boneseeking radiopharmaceutical since the half life (11.4 days) is about three times that of ²²⁴Ra, allowing a deeper incorporation into the matrix of the bone surfaces before decay occurs. Also, perhaps even more important, the radon daughter radon-219 has a short half-life (3.9 seconds), which should diminish translocation in, or as a result from the radon step. Three of the four α-particles emitted during decay of ²²³Ra and daughter nuclides are emitted immediately following ²²³Ra transformation (Seelman-Eggebert et al., 1981), i.e., of the first three transformations following ²²³Ra, the 3.9 second ²¹⁹Rn alpha decay is the one with the longest half life (Table 1). The last α-emitter in the ²²³Ra chain, ²¹¹Bi (t_(1/2)=2.15 min) follows the decay of the β-emitter lead-211 (t_(1/2)=36.1 min) and may therefore show some translocation. However, if the precursor, lead-211, is trapped inside of the bone matrix, also the last α-particle in the ²²³Ra series may be delivered to the bone surface area. In addition α-particles are high linear energy transfer (high-LET) radiation that is extremely cytotoxic to mammalian cells (Hall, 1994; Ritter et al., 1977). An α-particle emitting radiation source localized in target tissue can deliver radiation to a smaller target area, thus reducing normal tissue exposure compared to β-emitters.

[0010] The present invention relates to the preparation and the use of the “calcium analogue” alkaline-earth radionuclide radium-223 for the targeting of calcified tissues, e.g., bone and a physiological acceptable solution comprising ²²³ Ra.

[0011] In this patent application the inventors have invented a novel use of ²²³Ra, i.e., as an α-emitting radiopharmaceutical for targeting of calcified tissues, e.g., bone surfaces and osseous tumor lesions. As indicated by the properties of the radionuclide(s) as well as the experimental examples presented in the present patent application, radium-223 can be suitable as a bone seeking radio-pharmaceutical. As an example, the invention may be used for prophylactic cancer treatment by delivering a focused dose to bone surfaces in patients with a high probability of having undetected micrometastases at bone surfaces. Another example of its potential use would be in the treatment of painful osseous sites in a similar fashion as the previously described β- and electron emitting radiopharmaceuticals for bone pain palliation.

[0012] Radium-223 localized onto the bone surfaces and/or in calcified tumors can, together with its daughter nuclides, deliver an intense and highly local dose of α-particles with less bone marrow dose compared to currently used β-emitting and/or electron emitting radiopharmaceuticals. Skeletal diseases, e.g., primary or metastatic cancer to the bone may be treated with the ²²³Ra radiopharmaceutical.

[0013] The present invention includes the use of the nuclide as a cationic species and/or associated to a chelator or another form of a carrier molecule with affinity for calcified tissues. This also includes, but are not limited to the combination of radium-223 with a chelator that can be subsequently conjugated to a molecule with affinity for calcified tissues. The intent is to use the radioisotope to generate a cascade of α-particles on bone surfaces and/or in calcified tumors for the palliation of pain caused by various diseases and/or for the prophylactic use against possible minimal disease to the skeleton, and/or also for the therapeutic treatment of established cancer to the bone. The diseases where the radioisotopes could be used includes, but are not limited to skeletal metastases of prostate-, breast-, kidney- and lung cancer as well as primary bone cancer and also multiple myeloma.

[0014] Radium-223 solutions are prepared for use in the targeting of calcified tissues or for bone surface irradiation. The following examples are showing a high and selective uptake of the ²²³Ra in bone with very little relocalization of daughter nuclides. This shows that bone surfaces can be sterilized to inactivate microscopical deposits of cancer cells and also that calcified cancerous lesions can be irradiated either for palliation or therapy with this isotope. The compound differs from other commonly used radiopharmaceuticals with bone affinity because the main dose component comes from α-particles which has a much shorter range compared to the frequently used beta and electron emitters. Therefore the dose delivered to red bone marrow can be significantly reduced with this new compound, i.e., myelotoxicity is likely to be reduced. Radium-223 differs from the previously used medical radionuclide radium-224 in the following: (1) ²²³Ra has a significantly longer half-life affecting better bone to soft tissue ratios because a significantly larger fraction of this isotope would be eliminated from the soft tissues before decay occurs. (2) Longer half life also allows a deeper incorporation of the radionuclide into the bone surfaces as the bone synthesis progresses, potentially improving retention of daughter isotopes which may otherwise translocate because of chemical diffusion and nuclear recoil. (3) Also the shorter half life of the ²¹⁹Rn from ²²³Ra compared to the ²²⁰Rn from ²²⁴Ra, ensures less translocation of daughter nuclides from the ²²³Ra series.

[0015] The ²²³Ra salt or derivative thereof will be administered to a mammal, such as a human, in need thereof by all available administration routes, such as oral, subcutaneous, intravenous, intraarterial or transcutane. Preferably the active compound is administered by injection or infusion.

[0016] Oral administration is performed by use of tablets, capsules, powders or in liquid form, such as suspension, solution, syrup or emulsion. When formed into tablets conventional expicients, lubricating agents and binding agents are used. When administered as liquids conventional liquid carriers are used. When administered as injection or infusion solutions the carrier is preferably isotonic saline, with or without agent(s) to stabilize the radium cation to prevent precipitation of radium salts or insoluble complexes.

[0017] The active principle according to the invention could be used both in prophylactic, palliative and therapeutic treatment of non-malignant and malignant diseases affecting bones and soft tissues. The malignant diseases are selected from the group consisting of prostate cancer, breast cancer, kidney and urinary cancer, primary bone cancer, lung cancer and multiple myeloma, and the non-malignant disease are selected from the group consisting of autoimmune diseases affecting joints and skeleton, e.g. rheumatoid arthritis, schleroderma and spondyloartropathies.

[0018] The physiologically acceptable preparation for in vivo administration according to the present invention comprises dissolved radium-223 salt, with or without a single or a combination of several cations, as stabilizing alkaline earth metal cation analogue carrier, with or without an agent to prevent precipitation and/or generation of colloids, in addition to pharmacologically acceptable carriers and adjuvans. The cation acting as stabilizing alkaline earth metal cation can be selected from the group consisting of magnesium, calcium and strontium. Furthermore, the agent to prevent precipitation and/or generation of colloids is a carboxylic acid or a combination of carboxylic acids, such as oxalic acid, oxaloacetic acid, tartaric acid, succinic acid, malic acid and malonic acid. The concentrations of the compounds in the preparation will generally be less than the individual LD 50 dose, for example less than 20% of the LD 50 dose, and thus vary for the different components. The activity of ²²³Ra will be dependent upon the type and route of administration and the underlying condition or disease and will vary between approximately 50 kBq to approximately 10 MBq, administered in single or multiple doses for mammals, such as for example humans.

[0019] According to the invention radium-223 is furthermore used to produce a pharmaceutically active preparation to treat non-malignant and malignant diseases affecting bone, bone surfaces and soft tissues, both palliative and therapeutically.

[0020] The preparation is administered to the mammal, such as humans or animals, i.e. dogs, in need thereof, in a palliative or therapeutically effective amount.

[0021] According to the invention radium-223 can be used in a combination therapy, wherein the ²²³Ra preparation is combined with the following classes of treatment; chemotherapy including bisphosphonates, surgery, external beam irradiation, low-LET radiation emitting bone seeking radiopharmaceuticals, and hormonal treatment.

[0022] The invention is furthermore directed to a kit including ²²³Ra produced according to the inventive method, cations as stabilizing alkaline earth metal cation analogue carrier according and an agent to prevent precipitation and/or generation of colloids in addition to pharmaceutically acceptable carriers and suitable administration equipment.

[0023] In the following the present invention is described in detail by examples which in no way is intended to limit the scope of the invention as described by the enclosed claims.

[0024] Table 1 presents the physical properties of radium-223 and its daughter nuclides (Ekström et al., 1989). The decay of the ²²³Ra and its daughters causes the emissions of four α-particles. Such a cascade of α-particles can deliver a large radiation dose to a limited volume. Radium-223 therefore possesses extreme cytotoxicity, also compared to most α-emitters (Howell et al, 1997).

[0025] The following shows the Radium-223 and its daughters decay series (half life and mode of decay in brackets): ²²³Ra (11.4 d., α)

²¹⁹Rn (3.9 s., α)

²¹⁵Po (1.8 ms., α)

²¹¹Pb (36,1 min.,β⁻)

²¹¹Bi (2.15 min., α)

²⁰⁷T1(4,8 min., β⁻)

²⁰⁷Pb(stable) TABLE 1 Emittance from ²²³Ra and daughters*. Nuclide ²²³Ra ²¹⁹Rn ²¹⁵Po ²¹¹Pb ²¹¹Bi ²⁰⁷T1 α-Energy 5.64 MeV 6.75 MeV 7.39 MeV 6.55 MeV β-Energy 0.47 MeV 0.47 MeV (max) Energy 0.207 0.248 0.271 ≦0.017 0.24 ≦0.017 Fraction.^(#)

[0026] The combined energy from the emitted radiation associated with the complete decay of ²²³Ra and daughters: ˜27.5 MeV

[0027] Fraction of energy emitted as α-particles: ≧96%

[0028] Fraction of energy emitted as β-particles: ≦3%

[0029] Some gamma radiation (<0,3 MeV total) is also emitted during decay and can be used to determine the quality and quantity of isotopes in samples using gamma spectroscopy. E.g. radium-223 has a characteristic gamma peak at 154.19 keV (5.59% abundance), radon-219 has a peak at 401.78 keV (6,6%) and bismuth-211 has a 351.0 keV peak (12.8%) (Ekstrom et al., 1989). These can be used to determine if redistribution occurs for daughter isotopes in vivo. Also ²²³Ra has a 269.41 keV peak with 13.6% abundance, but this may be difficult to distinguish from a 271.23 keV peak, with 9.9% abundance of ²¹⁹Rn.

[0030] Production methods has been described for Radium-223 (Atcher et al., 1989; Howell et al., 1997). ²²³Ra is a member of a natural radioactive family originating from U (t_(1/2)=7×10⁸ y.) via ²³¹Th (t_(1/2)=25.6 y.) and the sequence ²³¹Th→²³¹Pa (t_(1/2)=3.3×10⁴ y.)→²²⁷Ac (t_(1/2)=21.7 y.)→²²⁷Th (t_(1/2)=18.7 d.)→²²³Ra (11.4 d.). Atcher et al. (1989) used a cation exchange system (Bio-rad AG 50) to produce ²²³Ra from ²²⁷Ac. Howell et al. (1997) used the ²²⁶Ra(n,γ)²²⁷Ra nuclear reaction to produce ²²³Ra. ²²⁷Ra(t_(1/2)=42 min) is rapidly transformed into ²²⁷Ac (t_(1/2)=21.77 years) which may be separated by different methods from the ²²⁶Ra target material. Howell et al (1997) separated the ²²⁷Ac chemically from a target solution. After that was ²²⁷Ac, together with its daughter products, transferred to an anion exchange column that retained ²²⁷Th, while the mother and daughter of this nuclide was eluted. Ten days later ²²³Ra could be eluted from the ion exchange column. If clinical batches were to be prepared by use of the generator principle, the application of ion exchange columns based on an organic backbone may be suboptimal because radiolysis may prevent long term multiple use of a radium generator based on this type of materials (Atcher et al., 1989).

[0031] Recently new materials have been developed, and are now commercial available, that are useful for separation of actinide radionuclides (selectivity for f-elements versus alkaline earth elements). These are based on silica particles covalently bound to or impregnated with active groups. Columns can be prepared using this material allowing the elution of some elements at conditions that can retain other elements. It would also be possible to use the active groups for the separation in wet/wet extraction systems using an organic and an aqueous phase.

EXAMPLES

[0032] In the following Example 1 ²²³Ra was produced. The novel method according to the invention for producing ²²³Ra for biomedical uses comprises both columns of inorganic matrix and liquid/liquid systems. A generator column containing a methane bis-phosphonic acid derivative on an inorganic matrix or the method can as well comprise a step of liquid/liquid extraction procedure in which one or more P,P′ di-esterified methylene bis-phosphonic acid derivates are used as phase transfer agents.

[0033] In the method the generator column containing P,P′ di-octyl methane bis-phosphonic acid on a silica matrix and the liquid/liquid extraction procedure is performed using P,P′ di-octyl methylene bis-phosphonic acid or P,P′ di(2-ethyl-hexyl) methane bis-phosphonic acid or combinations thereof as phase transfer agents. The prosedure with respect to the generator column is performed by using mineral acids which after neutralization is capable of giving physiologically compatible solutions of their salts, preferably nitric acid or hydrochlorid acid. The concentration of said mineral acids being in the range of 0.01 to 8M, more preferably between 0.1 and 2M, most preferably between 0.5 and 1M. The liquid/liquid extraction step is performed using a water phase consisting of a mineral acid, preferably nitric acid or hydrochloric acid, the concentration of which being in the range of 0.01 to 8M, more preferably between 0.1 and 2M most preferably between 0.8 and 1.5M.

Example 1

[0034]²²⁷Ac and ²²⁷Th were isolated from a ²³¹Pa source prepared 27 years earlier (Sample was provided by Radiochemistry Group, Department of Chemistry, University of Oslo, Norway), by use of an f-element selective extraction chromatographic resin. The purified ²²⁷Ac and ²⁷⁷Th were subsequently adsorbed onto another f-element selective extraction chromatographic resin and used as a cow for ²²³Ra. The latter material has been used by Wu et al. (1997) for construction of a generator for ²¹³Bi based on²²⁵Ac.

[0035] Methods: A sample of the ²³¹Pa source (with daughters) in an aqueous solution of 5 M H₂SO₄ and 1 M HF, was diluted 10 times with 1 M HCl. The solution was loaded onto a column of 3 mm inner diameter and length of 70 mm containing TRU-resin (EiChroM Industries, Darien, Ill., USA), which had been pre-equilibrated with 1 M HCl. ²³¹Pa was retained on the column while ²²⁷Ac, ²²⁷Th, and ²²³Ra was eluted partly by the loading procedure and partly by washing the column with additional 10 ml of 1 HCl. After this a ²²³Ra generatior was prepared by using a modification of the column packing technique described by Wu et al. (1997). A 3×50 mm column of Silica Actinide Resin (EiChroM, Darien, Ill., USA) consisting of P,P′ di-octyl methane bis-phosphonic acid (DIPEX, EiChroM Industries, Darien, Ill., USA) on silica particles with a diameter in the range of 20-50 μm was prepared and preconditioned with 1 M HCl. Approximately one half of the resin was then removed from the column and mixed with the eluate from the TRU-resin column.

[0036] The eluate containing ²²⁷Ac, ²²⁷Th and ²²³Ra was thereafter loaded onto 3 mm i.d. and 50 mm long column containing Actinide-resin (Ac-resin) on 30-50 μm silica (EiCroM Industries, Darien Ill., USA). Briefly, the column had been prepared according to the method of Wu et al. (1997). After preconditioning the column with 1 M HCl, half of the material was removed and mixed with the eluate from the preceding step.

[0037] After 4 hours of gentle agitation at room temperature, the slurry containing the radionuclides was loaded onto the column. Finally, the column was washed with 5 ml of 1 M HCl. The column was retaining ²²⁷Ac and ²²⁷Th while ²²³Ra could be eluted with a few ml of either HCl or HNO₃, without any significant breakthrough of its parent and grandparent radionuclides. If desired, a subsequent purification step could be added by simply eluting the ²²³Ra eluate through a second AC-resin column to remove any traces of mother and grandmother nuclides. The HCl solution containing the ²²³Ra could be diluted in a buffer, sterile filtered and used as such. Alternatively, the purified ²²³Ra could be concentrated before use by loading the HCl solution onto a 2 mm i.d. and 25 mm long column containing a resin, e.g., AG 50W-X4-16 (Bio-Rad, Richmond, Calif., USA). Thereafter the ²²³Ra could be eluted nearly quantitatively by a small volume of 6 M HNO₃. The HNO₃ could thereafter be evaporated of and the residue could be resolved in a solution that could subsequently be sterile filtered.

[0038] Radioactivity quality and quantity measurements were performed either using Ge-detector (Canberra, Meriden, Conn., USA) combined with an amplifier and bias supply from EG&G Ortec (Oak Ridge, Tenn., USA) for gamma spectroscopy and/or a Canberra (model 7404-0 1 A) combined with an EG&G Ortec for alpha spectroscopy.

[0039] Results: In the TRU-resin column, ²³¹Pa was quantitatively retained, i.e., the breakthrough was less than the detection limit of 0.5% compared to the daughter activity. Above 90% of the ²²⁷Ac and ²²⁷Th was collected in the eluate from the TRU-resin. For the AC-resin, multiple experiments indicated typical yields of 60-85 kBq ²²³Ra per 100 kBq of ²²⁷Th in the column (also named cow or generator) in the first few ml of stripping solution. The breakthrough of ²²⁷Ac and ²²⁷Th was determined to be less than (limited by detection capability) 4×10⁻³% compared to ²²³Ra. It should be noted that the described separation methods could also be used with the ²²⁷Ac produced from ²²⁶Ra via ²²⁶Ra (n, γ)²²⁷Ra→²²⁷Ac.

[0040] Conclusion: A set of methods is described for the production of ²²³Ra ensuring a high yield and a high purity useful for biological applications. Its distinction being the greater facilitation of routine production of clinically relevant activity levels of ²²³Ra from ²²⁷Ac. This is performed using a generator column based on a silica matrix (Wu et al., 1997) as compared to previously presented procedures involving more radiolytic sensitive ion-exchange resins containing organic matrixes (Atcher et al., 1989).

Example 2

[0041] The biodistribution of radium-223 prepared as described in Example 1 was studied.

[0042] Methods: Young male Balb/C mice with a body weight of 19-21 g were injected with 9 kBq of ²²³Ra in 150 μl of isotonic saline. Groups of five animals were sacrificed and dissected at 6 h and 3 days after injection. Sample weight was measured and samples were counted using (A) a “well type” NaI scintillation crystal (Harshaw Chemie BV, De Meern, Holland) combined with a Scaler Timer ST7 (NE Technology Ltd, Reading, UK) digital unit, (B) a Beckman LS 6500 (Beckman Instruments Inc. Fullerton, Calif., USA). Relative abundances of radionuclides were studied in blood, liver, kidney, and in standard samples with mother/daughter in equilibrium, using a Ge-detector (Canberra, Meriden, Conn., USA) combined with an amplifier and bias supply from EG&G Ortec (Oak Ridge, Tenn., USA).

[0043] Results: The biodistribution data is presented in Table 2. The data shows that ²²³Ra was selectively concentrated in bone compared to soft tissues. While all the soft tissue values were reduced between 6 h and 3 days after injection, the bone values increased with time. Femur to blood ratios increased from 129 to 691 from 6 h to 3 days. Spleen had the highest retention measured among the soft tissues, but the femur to spleen ratio also increased with time from 6.4 to 23.7 between 6 h and 3 days after injection. TABLE 2 Biodistribution of radium-223 in Balb/C mice presented as % of injected dose per gram. Tissue 6 hours 3 days femur 25.86 ± 1.99  34.55 ± 7.87  blood 0.20 ± 0.23 0.05 ± 0.10 kidney 4.04 ± 0.33 0.38 ± 0.08 liver 0.89 ± 0.18 0.22 ± 0.32 lung 0.59 ± 0.56 0.06 ± 0.07 muscle 0.72 ± 0.39 0.30 ± 0.16 heart 0.10 ± 0.10 0.06 ± 0.07 brain 0.04 ± 0.01 0.12 ± 0.12 spleen 4.06 ± 1.4  1.46 ± 0.54 small intestine 0.79 ± 0.26 0.04 ± 0.03 large intestine 2.30 ± 0.60 0.13 ± 0.02

[0044] Based on gamma spectroscopy data no significant difference in relative distribution of radium-223 and its daughters, as determined by abundance of ²¹¹Bi, could be observed in the bone and most soft tissues. The ratio of ²¹¹Bi:²²³Ra was in the spleen at the 6 hour point on average 54% compared to a standard solution. In liver and kidneys on the other hand, the ²¹¹Bi :²²³Ra ratios in the samples were on the average 256 and 207% of the standards respectively. This indicates that some translocation occurred in the soft tissues. Also the ²¹¹Bi activity in soft tissues was in general very low compared to bone activity of this nuclide. The ²¹¹Bi in the soft tissues may have been generated from ²²³Ra present in soft tissues.

[0045] Conclusion: Excellent bone to normal tissue radioactivity ratios were obtained with ²²³Ra and daughters, indicating a significant potential for the targeting of calcified tissues with this radionuclide series.

Example 3

[0046] To examine if there was a difference in radioisotope retention between radium-223 and bismuth-211 in bone samples, gamma spectroscopic data for bone versus a standard solution with ²²³Ra and daughter radionuclides in equilibrium was studied.

[0047] Methods: Gamma spectroscopy with a germanium detector (Canberra, Meriden, Conn., USA) was performed on samples of femur from mice immediately after sacrificing and dissecting the animals. Samples of a standard solution of ²²³Ra and daughter radionuclides in equilibrium were studied. The distinct gamma peaks at 351.0 keV (²¹¹Bi) and 154.2 keV (²²³Ra) were used. A Localization Index (LI) was determined as follows:

LI=(B_(Bi)/S_(Bi))/(B_(Ra)/S_(Ra))

[0048] E.g., B_(Bi)—²¹¹Bi count rate in bone; S_(Ra)—²²³Ra count rate in standard

[0049] Gamma spectra from five samples from the 6 h group and the 3 days group respectively were compared, to five and three samples from the standard solution respectively, using Student t-test for data columns.

[0050] Results: The LI values were on average 0.85 (P=0.059) at the 6 h point and 0.97 (P=0.749) at the 3 day point. However, the differences were not significant with respect to the P=0.05 level for the data sets.

[0051] Conclusion: Even for the radionuclide representing the fourth transformation in the series from ²²³Ra, the ²¹¹Pb-transformation, the retention in bone was similar to that of ²²³Ra.

Example 4

[0052] To study potential release of daughter isotopes after ²²³Ra was incorporated in bone, due to either nuclear recoil or diffusion processes, femurs from five animals killed 6 h, and 5 animals killed 3 days after injection were examined.

[0053] Methods: The bones were cleaved longitudinally, to expose the red marrow (spongious) areas, and thereafter cut into small fragments of less than 3 mg. Thereafter the samples were washed with Dulbeccos PBS (Sigma-Aldrich CO. LTD., Irvine, UK) using centrifugation. The supernatant was removed, mixed with scintillation liquid (Insta-Gel 11 plus, Packard BioScience BV, Groningen, The Netherlands) and counted on a scintillation counter (Beckman Instruments Inc. Fullerton, Calif., USA). After one day sample counting was repeated. A difference in counts after correcting for ²²³Ra decay between the two measurements was used as indication of release of daughter nuclide(s) from bone matrix.

[0054] Results: Animals killed after 6 hours showed some release of activity from bone. Compared to the total activity in bone an average of 1.8% was dissolved in PBS during washing. When the washing solutions were counted again after 12 h the activity then were only on average 0.2% of the bone sample. This indicates that some translocation of daughter isotopes had occurred but to a very small degree (probably for less than 2% of daughter isotopes). Animals killed after 3 days showed no significant counts compared to the background in the washing solution after washing. This indicates that if translocation occurred, it was below the detection limit, which was estimated to be less than 1% of the total bone radioactivity.

[0055] Conclusions: Based on the extractable radioactive fraction from finely fragmented bone samples it is indicated that daughter nuclide release (translocation) from bone matrix is low for the radium-223 series.

Example 5

[0056] It has been developed animal models with experimental metastasis pattern resembling those frequently observed in human patients (Engebraaten and Fodstad, 1999). One of these models consists of MT-1 cells injected intracardially into nude rats and is characterized by the consistent development of hind leg paralysis in the animals. Treatment (seven days after tumour cell inoculation) with the chemotherapeutics cisplatin or doxorubicin did not improve survival. Dissection and microscopic examination of the spine from animals affected by tumours revealed large masses of tumour cells replacing normal bone marrow and eroding the bony part of the spine.

[0057] The skeletal involvement in the above developed model made it suitable to demonstrate the therapeutic potential of ²²³Ra according to the invention against skeletal metastases.

[0058] Method: The therapeutic potential of radium-223 was studied in the MT-1/nude rat model where animals were inoculated with 1×10⁶ MT-1 human breast cancer cells by injection into the left ventricle of the heart as described (Engebraaten and Fodstad, 1999). These animals usually develop paralysis caused by growth of tumours in the spine. Groups of 4 and 5 animals each were then treated seven days later by receiving an intravenous injection of 200 μl of a vehicle solution without or with 10 kBq of radium-223 according to the invention.

[0059] Results: The group of four animals treated with vehicle solution alone experienced paralysis affected by tumour growth in the spine and was sacrificed between 20-25 days (means 22,25 days) after tumour cell inoculation. In the group of five animals receiving vehicle solution containing ²²³Ra one animal had paralysis after 26 days, one after 40 days and one after 64 days while the two remaining animals lived throughout the experimental follow-up period of 90 days after tumour cell inoculation, without showing signs of paralysis.

[0060] Conclusion: ²²³Ra demonstrated a significant anti-tumour effect in animals with skeletal metastases.

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1. Method to produce radium-223 for biomedical uses, characterized in loading a mother nuclide on generator column containing AC-resin on an inorganic matrix, or comprising a step using AC-resin in a liquid/liquid extraction system.
 2. Method according to claim 1, characterized in that the generator column contains a methane bis-phosponic acid derivative on silica matrix and in the step of liquid/liquid extraction one or more P,P′ di-esterified methylene bis-phosphonic acid derivatives or combinations thereof are used as phase transfer agents.
 3. Method according to claim 2, characterized in that the generator column contains P,P′ di-octyl methane bis-phosphonic acid on a silica matrix and in the step of liquid/liquid extraction P,P′ di-octyl methylene bis-phosphonic acid or P,P′ di(2-ethyl-hexyl)methane bis-phosphonic acid or combinations thereof are used as phase transfer agents.
 4. Method according to claim 1-3, characterized in that the generator column contains mineral acids which after neutralization gives physiological compatible solutions of their salts, preferably nitric acid or hydrocloric acid, and in the step of liquid/liquid extraction it is used a water phase consisting of a mineral acid, preferably nitric acid or hydrochloric acid.
 5. Method according to claim 4, characterized in that the concentration of the mineral acid in the said column is 0.01M-8M, preferably 0.1M-2M, more preferably 0.5M-1M, and the concentration of the mineral acid in the liquid/liquid extraction is 0.01M-8M, preferably 0.1M-2M, more preferably 0.8M-1.5M.
 6. Physiologically acceptable preparation for in vivo administration, characterized in comprising dissolved radium-223 salt, with or without a single or a combination of several cations as stabilizing alkaline earth metal cation analogue carrier, with or without an agent to prevent precipitation and/or generation of colloids, in addition to pharmacologically acceptable carriers and adjuvans.
 7. Preparation according to claim 6, characterized in that the cation acting as stabilizing alkaline earth metal cation are selected from the group consisting of magnesium, calcium and strontium.
 8. Preparation according to claim 6-7, characterized in that the agent to prevent precipitation and/or generation of colloids is a carboxylic acid or a combination of carboxylic acids.
 9. Preparation according to claim 8, characterized in that the carboxylic acids are selected from the group containing oxalic acid, oxaloacetic acid, tartaric acid, succinic acid, malic acid and malonic acid.
 10. Preparation according to claims 4-6, characterized in that it is prepared for injection, infusion or ingestion, or a combination thereof.
 11. Use of radium-223 to produce a pharmaceutically active preparation to treat diseased bone and bone surfaces.
 12. Use according to claim 11 wherein the preparation is used in a combination therapy with another therapeutically active component, such as but not limited to, chemotherapy including biphosphonates, surgery, external beam irradiation, low-LET radiation emitting bone seeking radiopharmaceuticals and hormonal treatment.
 13. Use according to claims 11-12, wherein the preparation is used for therapy and/or palliation related to non-malignant and malignant diseases affecting bones and/or soft tissues.
 14. Use according to claims 11-13, wherein the malignant diseases are selected from the group consisting of prostate cancer, breast cancer, kidney and urinary cancer, primary bone cancer, lung cancer and multiple myeloma.
 15. Method for prophylactic or therapeutical treatment of non-malignant or malignant disease affecting bones and soft tissues in a mammal, characterized in comprising administrating to the mammal in need thereof a palliative or therapeutically effective amount of the preparation according to claims 6-10.
 16. Method according to claim 15, characterized in that it is administered to the mammal a prophylactic effective amount.
 17. Method according to claims 14-16, characterized in that the mammal is a dog or a human.
 18. Kit, characterized in containing ²²³Ra produced according to claims 1-5, cations as stabilizing alkaline earth metal cation analogue carrier according to claim 7, and an agent to prevent precipitation and/or generation of colloids according to claims 8-9, pharmaceutically acceptable carriers and suitable administration equipment. 